Gene-specific Copy Number Variation Probe-F7
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| Catalog: |
CNVFP-F7-04926 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (F7). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
F7 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to F7 genes. This product achieves the purpose of detection by hybridizing with the F7 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Coagulation Factor VII |
| Gene Summary [Provided by RefSeq] |
This gene encodes coagulation factor VII which is a vitamin K-dependent factor essential for hemostasis. This factor circulates in the blood in a zymogen form, and is converted to an active form by either factor IXa, factor Xa, factor XIIa, or thrombin by minor proteolysis. Upon activation of the factor VII, a heavy chain containing a catalytic domain and a light chain containing 2 EGF-like domains are generated, and two chains are held together by a disulfide bond. In the presence of factor III and calcium ions, the activated factor then further activates the coagulation cascade by converting factor IX to factor IXa and/or factor X to factor Xa. Defects in this gene can cause coagulopathy. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing to generate mature polypeptides. [provided by RefSeq, Aug 2015] |
| Gene Symbol |
F7 |
| Location |
13q34 |
| Chromosome |
Chromosome13 |
| Coordinates |
This gene maps to 113760104-113774995 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-F7-04926-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-F7-04926-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-F7-04926-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-F7-04926-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-F7-04926-AQ |
467nm |
418nm |
|
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